Label: LIQUID CALLUS REMOVER- salicylic acid liquid

  • NDC Code(s): 56104-501-00
  • Packager: Premier Brands of America Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • Active ingredient

    Salicylic acid 17% w/w

  • Purpose

    Corn and callus remover

  • Uses

    • for the removal of corns and calluses
    • relieves pain by removing corns and calluses
  • Warnings

    For external use only.

    Flammable

    • keep away from fire or flame

    Do not use

    • on irritated skin
    • on any area that is infected or reddened
    • if you are a diabetic or if you have poor blood circulation

    When using this product

    • if product gets into the eye, flush with water for 15 minutes
    • avoid inhaling vapors
    • cap bottle tightly and store at room temperature away from heat

    Stop and ask a doctor if

    discomfort persists

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wash the affected area and dry thoroughly
    • apply one drop at a time with applicator to sufficiently cover each corn/callus
    • let dry
    • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
    • may soak corn/callus in warm water for 5 minutes to assist in removal
  • Other information

    • store between 20° to 25°C (68° to 77°F)
    • avoid surrounding skin when applying product
    • close tightly to prevent solidification
    • wipe top of bottle clean after each use
    • do not allow to come into contact with fabrics, floors, countertops or other surfaces -- will stain
  • Inactive ingredients

    camphor, castor oil, ethanol, ethyl ether, nitrocellulose

  • Questions?

  • Principal Display Panel

    EndZone

    LIQUID

    CALLUS

    REMOVER

    SALICYLIC ACID 17% / CORN & CALLUS REMOVER

    Safely removes corns & calluses

    0.33 FL OZ (9.8 mL) Image 1Image 2

  • INGREDIENTS AND APPEARANCE
    LIQUID CALLUS REMOVER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID170 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PYROXYLIN (UNII: KYR8BR2X6O)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56104-501-001 in 1 CARTON09/11/2023
    19.8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03009/11/2023
    Labeler - Premier Brands of America Inc. (117557458)
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